Show simple item record

FieldValueLanguage
dc.contributor.authorRockett, Rebecca J.en_AU
dc.contributor.authorDraper, Jennyen_AU
dc.contributor.authorGall, Mailieen_AU
dc.contributor.authorSim, Eby M.en_AU
dc.contributor.authorArnott, Aliciaen_AU
dc.contributor.authorAgius, Jessica E.en_AU
dc.contributor.authorJohnson-Mackinnon, Jessicaen_AU
dc.contributor.authorFong, Winkieen_AU
dc.contributor.authorMartinez, Elenaen_AU
dc.contributor.authorDrew, Alexander P.en_AU
dc.contributor.authorLee, Clementen_AU
dc.contributor.authorNgo, Christineen_AU
dc.contributor.authorRamsperger, Marcen_AU
dc.contributor.authorGinn, Andrew N.en_AU
dc.contributor.authorWang, Qinningen_AU
dc.contributor.authorFennell, Michaelen_AU
dc.contributor.authorKo, Dannyen_AU
dc.contributor.authorHueston, Lindaen_AU
dc.contributor.authorKairaitis, Lukasen_AU
dc.contributor.authorHolmes, Edward C.en_AU
dc.contributor.authorO’Sullivan, Matthew N.en_AU
dc.contributor.authorChen, Sharon C.-A.en_AU
dc.contributor.authorKok, Jenen_AU
dc.contributor.authorDwyer, Dominic E.en_AU
dc.contributor.authorSintchenko, Vitalien_AU
dc.date.accessioned2022-07-04T00:45:41Z
dc.date.available2022-07-04T00:45:41Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/2123/28985
dc.description.abstractCo-infections with different variants of SARS-CoV-2 are a key precursor to recombination events that are likely to drive SARS-CoV-2 evolution. Rapid identification of such co-infections is required to determine their frequency in the community, particularly in populations at-risk of severe COVID-19, which have already been identified as incubators for punctuated evolutionary events. However, limited data and tools are currently available to detect and characterise the SARS-CoV-2 co-infections associated with recognised variants of concern. Here we describe co-infection with the SARS-CoV-2 variants of concern Omicron and Delta in two epidemiologically unrelated adult patients with chronic kidney disease requiring maintenance haemodialysis. Both variants were co-circulating in the community at the time of detection. Genomic surveillance based on amplicon- and probe-based sequencing using short- and long-read technologies identified and quantified subpopulations of Delta and Omicron viruses in respiratory samples. These findings highlight the importance of integrated genomic surveillance in vulnerable populations and provide diagnostic pathways to recognise SARS-CoV-2 co-infection using genomic data.en_AU
dc.language.isoenen_AU
dc.subjectCOVID-19en_AUI
dc.subjectCoronavirusen_AUI
dc.titleCo-infection with SARS-CoV-2 Omicron and Delta variants revealed by genomic surveillanceen_AU
dc.typeArticleen_AU
dc.identifier.doi10.1038/s41467-022-30518-x


Show simple item record

Associated file/s

There are no files associated with this item.

Associated collections

Show simple item record

There are no previous versions of the item available.